Voltage-Regulated Water Flux through Aquaporin Channels In Silico

被引:68
作者
Hub, Jochen S. [1 ]
Aponte-Santamaria, Camilo [2 ]
Grubmueller, Helmut [2 ]
de Groot, Bert L. [2 ]
机构
[1] Uppsala Univ, Dept Cell & Mol Biol, Uppsala, Sweden
[2] Max Planck Inst Biophys Chem, Dept Theoret & Computat Biophys, D-37077 Gottingen, Germany
关键词
CRYSTAL-STRUCTURE; PERMEATION; AQPZ;
D O I
10.1016/j.bpj.2010.11.003
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Aquaporins (AQPs) facilitate the passive flux of water across biological membranes in response to an osmotic pressure. A number of AQPs, for instance in plants and yeast, have been proposed to be regulated by phosphorylation, cation concentration, pH change, or membrane-mediated mechanical stress. Here we report an extensive set of molecular dynamics simulations of AQP1 and AQP4 subject to large membrane potentials in the range of +/- 1.5 V, suggesting that AQPs may in addition be regulated by an electrostatic potential. As the regulatory mechanism we identified the relative population of two different states of the conserved arginine in the aromatic/arginine constriction region. A positive membrane potential was found to stabilize the arginine in an up-state, which allows rapid water flux, whereas a negative potential favors a down-state, which reduces the single-channel water permeability.
引用
收藏
页码:L97 / L99
页数:3
相关论文
共 9 条
[1]   Crystal structure of human aquaporin 4 at 1.8 Å and its mechanism of conductance [J].
Ho, Joseph D. ;
Yeh, Ronald ;
Sandstrom, Andrew ;
Chorny, Ilya ;
Harries, William E. C. ;
Robbins, Rebecca A. ;
Miercke, Larry J. W. ;
Stroud, Robert M. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (18) :7437-7442
[2]   Crystal structure of AqpZ tetramer reveals two distinct Arg-189 conformations associated with water permeation through the narrowest constriction of the water-conducting channel [J].
Jiang, JS ;
Daniels, BV ;
Fu, D .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (01) :454-460
[3]   From structure to disease: The evolving tale of aquaporin biology [J].
King, LS ;
Kozono, D ;
Agre, P .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2004, 5 (09) :687-698
[4]   Structural determinants of water permeation through aquaporin-1 [J].
Murata, K ;
Mitsuoka, K ;
Hirai, T ;
Walz, T ;
Agre, P ;
Heymann, JB ;
Engel, A ;
Fujiyoshi, Y .
NATURE, 2000, 407 (6804) :599-605
[5]  
Nedvetsky Pavel I, 2009, Handb Exp Pharmacol, P133, DOI 10.1007/978-3-540-79885-9_6
[6]   APPEARANCE OF WATER CHANNELS IN XENOPUS OOCYTES EXPRESSING RED-CELL CHIP28 PROTEIN [J].
PRESTON, GM ;
CARROLL, TP ;
GUGGINO, WB ;
AGRE, P .
SCIENCE, 1992, 256 (5055) :385-387
[7]   Structural basis of water-specific transport through the AQP1 water channel [J].
Sui, HX ;
Han, BG ;
Lee, JK ;
Walian, P ;
Jap, BK .
NATURE, 2001, 414 (6866) :872-878
[8]   Structural insights into eukaryotic aquaporin regulation [J].
Tornroth-Horsefield, Susanna ;
Hedfalk, Kristina ;
Fischer, Gerhard ;
Lindkvist-Petersson, Karin ;
Neutze, Richard .
FEBS LETTERS, 2010, 584 (12) :2580-2588
[9]   What makes an aquaporin a glycerol channel? A comparative study of AqpZ and GlpF [J].
Wang, Y ;
Schulten, K ;
Tajkhorshid, E .
STRUCTURE, 2005, 13 (08) :1107-1118